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FAM53B

family with sequence similarity 53 member B

HCNC Approved Symbol
FAM53B (HGNC:28968)
Genomic Coordinates
10:124,619,292 - 124,744,378 (10q26.13)
Synonyms
bA12J10.2, smp, KIAA0140
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 3 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

FAM53B - Gene browser | 3billion